pivaloyl chloride

CC(C)(C)C(=O)Nc1ncnc2c1ncn2[C@H]1CC=CO1
Reaction #1654
(R)-N-[9-(2,3-Dihydro-2-furanyl)-9H-purin-6-yl]-2,2-dimethylpropanamide
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ccc(NC(=O)C(C)(C)C)cn2)cc1
Reaction #2379
N-[6-[2-{6-(4-tert-butylphenylsulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yloxy}ethoxy]pyridin-3-yl]pivalamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(NC(=O)C(C)(C)C)cc1
Reaction #2599
title compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)CCNc1nc2cc(OC(=O)C(C)(C)C)ccc2c2c1C(=O)c1ccccc1-2
Reaction #3253
title compound
Ausbeute 83.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C(=O)Oc1ccc(CCNC(=O)OCc2ccccc2)cc1OC(=O)C(C)(C)C
Reaction #6000
desired compound
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)C(=O)NCCCSc1ccncc1.Cl
Reaction #6196
desired compound
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)C(=O)NCCCOc1ccncc1
Reaction #6237
desired compound
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)C(=O)Nc1cccc(C(F)(F)F)c1
Reaction #6521
solid
Ausbeute 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)C(=O)Nc1cc2c(O)nc[nH]c-2n1
Reaction #6620
4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine
Ausbeute 89.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(NC(=O)C(C)(C)C)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7657
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]-2,2-dimethylpropanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1CC(OC(=O)C(C)(C)C)CN1C(=O)OCc1ccccc1
Reaction #7751
desired product
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)C(=O)Nc1cccnc1
Reaction #7872
N-(pyridin-3-yl)-2,2-dimethylpropanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)C(=O)Nc1c(C(=O)c2cccnc2)oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
Reaction #8885
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1S(=O)(=O)NC(=O)C(C)(C)C
Reaction #11761
title compound
Ausbeute 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)C(=O)Nc1cnc(Br)cn1
Reaction #40275
title compound
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)C(=O)N1CCC2(CC1)CC(=O)Nc1ccccc12
Reaction #40673
19c
Ausbeute 79.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1CCN(C(=O)C(C)(C)C)CC1
Reaction #40674
20a
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](NC(=O)C(C)(C)C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41324
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]-2,2-dimethyl-propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCc1ccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)C(C)(C)C)cc1
Reaction #41332
N-[(1R,2S)-1-(4-ethylphenyl)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-propan-2-yl]-2,2-dimethyl-propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc2c(cnn2-c2ccc(F)cc2)cc1O[C@H](c1ccccc1)[C@H](C)NC(=O)C(C)(C)C
Reaction #41347
N-[(1R,2S)-1-[1-(4-Fluorophenyl)-6-methyl-indazol-5-yl]oxy-1-phenyl-propan-2-yl]-2,2-dimethyl-propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Seite 1Weiter